HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192583Generated: November 1, 2026
Trifluoromethanesulfonic anhydride → 3-Oxo-5-(trifluoromethyl)cyclohex-1-enyl trifluoromethanesulfonate
https://huagongshe.com/reaction/2192583
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | 5-(Trifluoromethyl)cyclohexane-1,3-dione | HCID 59226574 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Oxo-5-(trifluoromethyl)cyclohex-1-enyl trifluoromethanesulfonate | HCID 59226600 | — |
Reaction Steps
To a suspension of 5-(trifluoromethyl)cyclohexane-1,3-dione (1.0 eq) in DCM (0.23 M) was added TEA (1.2 eq) to give a clear solution. The mixture was cooled to 0° C. And then Tf2O (1.05 eq) in DCM was added dropwise. The reaction mixture was stirred at that temperature for 2 hours. The reaction mixture was diluted with DCM, and washed with water, aq. NaHCO3, brine, and was dried over MgSO4, filtered and concentrated to give 3-oxo-5-(trifluoromethyl)cyclohex-1-enyl trifluoromethanesulfonate, which was used to next step directly. LC/MS (m/z): MH+=313.0, Rt=1.02 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08329732B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-aa4cd7152f954714b98bc525f1561ec5 |
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| Source note | uspto-grants-2012_12 |
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